510(k) K973740 ยท ETD Tube, Tympanostomy
ROUND WINDOW E-CATH
| Applicant | Neuro-Biometrix, Inc., Englewood CO, US |
| Decision | Substantially Equivalent, Mar 23, 1998 |
| Received | Oct 1, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K973740
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.